An siRNA library screen identifies CYLD and USP34 as deubiquitinases that regulate GPCR-p38 MAPK signaling and distinct inflammatory responses

J Biol Chem. 2023 Dec;299(12):105370. doi: 10.1016/j.jbc.2023.105370. Epub 2023 Oct 20.

Abstract

G protein-coupled receptors (GPCRs) are highly druggable and implicated in numerous diseases, including vascular inflammation. GPCR signals are transduced from the plasma membrane as well as from endosomes and controlled by posttranslational modifications. The thrombin-activated GPCR protease-activated receptor-1 is modified by ubiquitin. Ubiquitination of protease-activated receptor-1 drives recruitment of transforming growth factor-β-activated kinase-1-binding protein 2 (TAB2) and coassociation of TAB1 on endosomes, which triggers p38 mitogen-activated protein kinase-dependent inflammatory responses in endothelial cells. Other endothelial GPCRs also induce p38 activation via a noncanonical TAB1-TAB2-dependent pathway. However, the regulatory processes that control GPCR ubiquitin-driven p38 inflammatory signaling remains poorly understood. We discovered mechanisms that turn on GPCR ubiquitin-dependent p38 signaling, however, the mechanisms that turn off the pathway are not known. We hypothesize that deubiquitination is an important step in regulating ubiquitin-driven p38 signaling. To identify specific deubiquitinating enzymes (DUBs) that control GPCR-p38 mitogen-activated protein kinase signaling, we conducted a siRNA library screen targeting 96 DUBs in endothelial cells and HeLa cells. We identified nine DUBs and validated the function two DUBs including cylindromatosis and ubiquitin-specific protease-34 that specifically regulate thrombin-induced p38 phosphorylation. Depletion of cylindromatosis expression by siRNA enhanced thrombin-stimulated p38 signaling, endothelial barrier permeability, and increased interleukin-6 cytokine expression. Conversely, siRNA knockdown of ubiquitin-specific protease-34 expression decreased thrombin-promoted interleukin-6 expression and had no effect on thrombin-induced endothelial barrier permeability. These studies suggest that specific DUBs distinctly regulate GPCR-induced p38-mediated inflammatory responses.

Keywords: PAR1; inflammation; p38 MAPK; thrombin; ubiquitin.

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Cell Line
  • Deubiquitinating Enzyme CYLD* / metabolism
  • Deubiquitinating Enzymes* / metabolism
  • Endothelial Cells* / metabolism
  • Gene Expression Regulation, Enzymologic
  • HeLa Cells
  • Humans
  • Interleukin-6 / metabolism
  • Phosphorylation / genetics
  • RNA, Small Interfering / metabolism
  • Receptor, PAR-1 / metabolism
  • Thrombin* / metabolism
  • Thrombin* / pharmacology
  • Ubiquitin / metabolism
  • Ubiquitin-Specific Proteases / metabolism
  • p38 Mitogen-Activated Protein Kinases / genetics
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • CYLD protein, human
  • Deubiquitinating Enzyme CYLD
  • Deubiquitinating Enzymes
  • Interleukin-6
  • p38 Mitogen-Activated Protein Kinases
  • Receptor, PAR-1
  • RNA, Small Interfering
  • TAB2 protein, human
  • Thrombin
  • Ubiquitin
  • Ubiquitin-Specific Proteases
  • USP34 protein, human